FDA PMA FDA Class 3 Approved 🇺🇸 United States

Aid, Surgical, Viscoelastic

PMA: P880031 · Supplement: S016 · Decision Feb 18, 2009
Classifications
1
FEI Numbers
27
Registration Numbers
27

Basic Information

Device Name
Aid, Surgical, Viscoelastic
Trade Name
HEALON D SODIUM HYALURONATE SOLUTION
PMA Number
P880031
Supplement Number
S016
Device Class
FDA Class 3
Product Code
LZP
Generic Name
AID, SURGICAL, VISCOELASTIC
Regulation Number
886.4275
Medical Specialty
Ophthalmic
Advisory Committee
Ophthalmic
Decision
Approved
Decision Code
APPR
Decision Date
February 18, 2009
Date Received
January 8, 2009
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

APPROVAL TO CHANGE THE PH PRODUCT SPECIFICATION RANGE FOR HEALON D FROM 7.1 ¿ 7.5 TO 6.8 ¿ 7.6.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LZP Aid, Surgical, Viscoelastic